WO1993025649A1 - Suds controlling composition comprising silicone and silica - Google Patents

Suds controlling composition comprising silicone and silica Download PDF

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Publication number
WO1993025649A1
WO1993025649A1 PCT/US1993/004924 US9304924W WO9325649A1 WO 1993025649 A1 WO1993025649 A1 WO 1993025649A1 US 9304924 W US9304924 W US 9304924W WO 9325649 A1 WO9325649 A1 WO 9325649A1
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WO
WIPO (PCT)
Prior art keywords
silica
suds controlling
controlling composition
composition according
surfactant
Prior art date
Application number
PCT/US1993/004924
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English (en)
French (fr)
Inventor
Athanasios Surutzidis
Roger Jeffery Jones
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to AU43894/93A priority Critical patent/AU4389493A/en
Priority to JP6501497A priority patent/JPH07507588A/ja
Priority to CA002137344A priority patent/CA2137344C/en
Publication of WO1993025649A1 publication Critical patent/WO1993025649A1/en
Priority to FI945732A priority patent/FI945732A/fi

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0034Fixed on a solid conventional detergent ingredient
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • B01D19/0409Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing Si-atoms
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/08Silicates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones

Definitions

  • the present invention relates to suds controlling compositions and stable liquid detergent compositions containing them.
  • Silicone oil and hydrophobic silica mixtures in finely dispersed form have been found to be particularly effective antifoam agents, and efforts have been directed towards increasing the stability of such agents upon prolonged storage in liquid detergent compositions containing them. However, it has found to be difficult to create and maintain the finely dispersed form of said antifoam agents in liquid detergent compositions, especially in a high ionic strength medium.
  • a suds controlling composition which has improved stability upon storage when incorporated into liquid detergents.
  • a stable liquid detergent composition comprising said suds controlling composition is provided.
  • a process is provided to obtain stable liquid detergent compositions comprising the suds controlling composition of the present invention.
  • the present invention provides suds controlling composition for inclusion in a detergent composition in liquid form, comprising a silicone oil/ silica antifoam agent and a dispersant characterised in that the silica is absorbed with a surfactant-containing solution.
  • the present invention also provides liquid detergent compositions comprising said suds controlling composition, surface-active agents and optionally other detergent ingredients.
  • the silicone oil/silica antifoam agent according to the present invention comprises a mixture of a silicone oil and solid silica.
  • silicone has become a generic term which encompasses a variety of relatively high- ⁇ olecular-weight polymers containing siloxane units and hydrocarbyl groups of various types.
  • silicone oil can be described as siloxanes having the general structure •'
  • n is from 20 to 2.000, and where each R independently can be an alkyl or an aryl radical. Examples of such substituents are methyl, ethyl, propyl, isobutyl, and phenyl.
  • Preferred polydiorganosiloxanes are polydimethylsiloxanes having trimethylsilyl endblocking units and having a viscosity at 25 : C of from 5 x 10 -5 m 2 /s to 0.1 m /s i.e. a value of n in the range 40 to 1500. These are preferred because of their ready availability and their relatively low cost.
  • Suitable silicone oils that can be used for the present invention are functional silicone oils.
  • Preferred functional silicone oils are anionic or cationic type of silicone oils.
  • the solid silica can be a fumed silica, a precipitated silica or a silica made by the gelformation technique.
  • the silica particles can be rendered hyrophobic by treating them with diaklylsilane groups and/or trialkylsilane groups either bonded directly onto the silica or by means of silicone resin.
  • a preferred silica comprises a hydrophobic silanated, most preferably tri ethylsilanated silica having a particle size in the range from 10 nanometer to 20 nanometer and a specific surface area above 50 m 2 /g.
  • the silica is further characterized, by a high absorption value.
  • the absorption can be expressed as Dibutylphtalate (DBP) number.
  • Porous silica suitable for the present invention is available under the trade name Sipernat (R) from Degussa.
  • the silicone oil/silica antifoam agents employed in the suds controlling composition suitable for to the present invention have an amount of silica in the range of 1 to 30%, more preferably from 1 to 20% by weight of the total weight of the silicone oil.
  • the silicone oil/silica antifoam agents as described hereinabove, must be present in the liquid detergent compositions in finely dispersed form in order to be effective. However, the particles of said antifoam agent present in the liquid detergent composition tend to coagulate upon storage.
  • the concept of "stability" as used herein is in the context of maintaining the silicone oil / silica antifoam agent in finely dispersed form.
  • the absorption of a surfactant-containing solution reduces the coalescence of the silicone oil/ silica antifoam particles so that stable detergent formulas can be prepared.
  • the surfactant-containing solution comprises a surfactant selected from an anionic, nonionic, ampholytic or zwitterionic surfactant.
  • the surfactant-containing solution comprises a nonionic surfactant.
  • a wide range of nonionic surfactants can be used.
  • Suitable nonionic surfactants are condensates of ethylene oxide with a hydrophobic moiety to provide a surfactant having a hydrophillic-lipophillic balance (HJ.B) in the range from 8 to 17, preferably from 8 to 17, preferably from 9.5 to 13.5, more preferably from 10 to 12.5.
  • HJ.B hydrophillic-lipophillic balance
  • Especially preferred nonionic surfactants of this type are the Cg-C 15 primary alcohol ethoxylates containing 3-8 moles of ethylene oxide per mole of alcohol, particularly the Ci ⁇ -C ⁇ primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol and the C 1 ⁇ c 14 primary alcohols containing 3-5 moles of ethylene x>xide per mole of alcohol.
  • the surfactants present in the surfactant-containing solution should be present at levels sufficiently high to ensure the wetting of the silica.
  • the level of surfactant that can be used should be such to maintain a free flowing powder.
  • the level of ethoxylated fatty alcohols with an HLB-value in the range of 9 to 13 is present from
  • the silica/silicone mixture further comprises ultra-fine particles, said particles having average particle sizes less than 0.1 micron.
  • Preferred particles to be added are silica particles.
  • a preferred silica is fumed nonporous silica. Exa pe of such silica is available under the trade name Aerosil R972 ex Degussa. Dispersant
  • the suds contolling composition of the present invention comprises a dispersing agent.
  • the dispersing agent disperses or helps disperse the silicone suds control agent uniformly so that stable, preferably homogeneous, detergent formulas can be prepared.
  • the dispersing agent is premixed with the antifoam agent prior to incorporation into the liquid detergent composition.
  • Suitable dispersing agents include materials such as ethylene oxide adducts of linear or arylphenols having from 8 to 20 carbon atoms per molecule, such as lauryl polyoxethylene glycol ether, stearyl polyoxyethylene, glycol ether, cetyl polyoxyethylene glycol ether, and nonylphenol polyoxyethylene glycol ether, and also ethylene oxide adducts of linear or branched onocarboxylic acids and having HLBs of greater than about 13.5, preferably greater than about 14.
  • such addition products have short hydrophylic chains containing 12 or preferably less carbon atoms and from about 8 to about 15 ethylene oxide units per molecule.
  • preferred dispersants are polyoxyethylene glycol sorbitan esters of polyoxyethylene glycol sorbital esters having HLB values of 14 or more, such as polyoxyethylene glycol sorbitan hexaoleate or polyoxyethylene sorbitol hexaoleate.
  • Additional examples of preferred dispersants are fatty acid nono-,di-, and/or polyglycerides and sodium or calcium stearoyl lactate, diglycerol stearate, and sorbitan monostearate.
  • the anti-foam agnet of the present invention can contain a single type of dispersant or mixtures of at least two different types of dispersants.
  • Suitable dispersants are commercial oxyethylated polyhydric alcohols or their derivatives or similar compounds having an active hydrogen atom, as well as fatty acid esters of glycerol or sorbitol.
  • Anionic emulsifiers such as sodium dodecylbenzene-sulphonate or sodium laurylsulphate, can also be used, but preferably with a solvent.
  • Preferred is an emulsifier mixture of oxyethylated fatty alcohol and oxyethylated triglyceride having an HLB value preferably in the range from about 14 to 16.
  • the preferred solvent for di ethylpolysiloxane is tetrameric or pentameric cyclomethicone.
  • Particularly preferred dispersants for use herein are cyclomethicone and C9-C11 linear chain alcohols ethoxylated with from about 7 to about 10 moles of ethylene oxide per mole of alcohol especially when the unreacted alcohol and monoethoxylated alcohol are removed and mixtures thereof.
  • Most preferred dispersants are silicone glycol copolymers, optionally in combination with cyclomethicone compounds. Examples of said mixtures which are commercially available are DC3225C manufactured by Dow Corning.
  • the weight ratio of dispersant to silica/silicone antifoam agent is preferably from 1:100 to 1:1, more preferably from 1:10 to 1:2.
  • the suds controlling composition of the present invention comprise the silicone oil/ silica anti-foam agent in the form of a dispersion in a water-soluble or water- dispersable organic carrier for incorporation into a detergent composition .
  • Suitable organic carriers are nonionic surfactants.
  • the nonionic surfactants are ethoxylated surfactants.
  • ethoxylated nonionic surfactants suitable herein have an average ethyleneoxy content in the range from 35% to 70% and especially from 50% to 62.5% by weight of the surfactant.
  • suitable nonionic surfactants include the condensation products of primary or secondary aliphatic alcohols having from 8 to 24 carbon atoms, in either straight chain or branched chain configuration, with from 2 to 18 moles of alkylene oxide per mole of alcohol.
  • the aliphatic alcohol comprises between 9 and 15 carbon atoms and is ethoxylated with between 2 and 9, desirably between 3 and 8 moles of ethylene oxide per mole of aliphatic alcohol.
  • alkoxylated nonionic surfactants having an average HLB in the range from 9.5 to 13.5, especially 10 to 12.5.
  • Highly suitable nonionic surfactants of this type are ethoxylated primary C9-15 alcohols having an average degree of ethoxylation from 2 to 9, more preferably from 3 to 8.
  • the compounds of the suds controlling composition are premixed before incorporation into the liquid detergent composition.
  • the suds controlling composition of the present invention is made by absorbing the surfactant into the pores of the silica which is then dispersed in the silicone oil.
  • the silicone oil dispersion can be mixed with the dispersant in a high shear mixer.
  • the high shear mix can be prepared using any conventional high shear mixing equipment.
  • the suds controlling composition of the present invention can also be incorporated in detergent additive products.
  • Such additive products are intended to supplement or boost the performance of conventional detergent compositions and may contain any of the components of such compositions.
  • the liquid detergent compositions comprising the suds controlling composition of the present invention is made by mixing the suds controlling composition together with detergent ingredients.
  • a variant of this process comprises a premix of the suds controlling composition with a carrier material. The premix is then mixed with the other detergent ingredients.
  • the liquid detergent compositions comprising the suds controlling composition can be provided having various ratios and proportions of the detergent ingredients.
  • the amount of suds controlling composition in the liquid detergent composition can be varied, depending upon the suds profile desired by the formulation.
  • the level of the suds controlling composition is preferable present from 0.8% to 3.0% by weight of the total detergent composition.
  • a liquid detergent composition comprising the suds controlling composition of the present invention mixed with detergent ingredients.
  • Detergent ingredients include surfactants, builders and optional detergent additives. A wide range of surfactants can be used in the detergent composition of the present invention.
  • anionic surfactants are particularly suitable herein, especially mixtures of sulphonate and sulphate surfactants in a weight ratio of from 5:1 to 1:2, preferably from 3:1 to 2:3, more preferably from 3:1 to 1:1.
  • Preferred sulphonates include alkyl benzene sulphonates having from 9 to 15, especially 11 to 13 carbon atoms in the alkyl radical, and alpha-sulphonated methyl fatty acid esters in which the fatty acid is derived from a C 1 2 ⁇ c 18 fa ty source preferably from a 16 ⁇ 1 8 fatty source.
  • the cation is an alkali metal, preferably sodium.
  • Preferred sulphate surfactants are alkyl sulphates having from 12 to 18 carbon atoms in the alkyl radical, optionally in admixture with ethoxy sulphates having from 10 to 20, preferably 10 to 16 carbon atoms in the alkyl radical and an average degree of ethoxylation of 1 to 6.
  • alkyl sulphates examples include tallow alkyl sulphate, coconut alkyl sulphate, and Ci4_i5 alkyl sulphates.
  • the cation in each instance is again an alkali metal cation, preferably sodium.
  • One class of nonionic surfactants useful in the present invention are condensates of ethylene oxide with a hydrophobic moiety to provide a surfactant having an average hydrophilic- lipophilic balance (HLB) in the range from 8 to 17, preferably from 9.5 to 13.5, more preferably from 10 to 12.5.
  • HLB hydrophilic- lipophilic balance
  • the hydrophobic (lipophilic) moiety may be aliphatic or aromatic in nature and the length of the polyoxyethylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • Especially preferred nonionic surfactants of this type are the C9-C15 primary alcohol ethoxylates containing 3-8 moles of ethylene oxide per mole of alcohol, particularly the C14-C15 primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol and the Ci2 ⁇ c 1 4 primary alcohols containing 3-5 moles of ethylene oxide per mole of alcohol.
  • Another class of nonionic surfactants comprises alkyl polyglucoside compounds of general formula
  • Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides.
  • nonionic surfactants are poly hydroxy fatty acid amide surfactants of the formula
  • R 1 is H, or R 1 is C-j ⁇ hydrocarbyl, 2-hydroxy ethyl, 2- hydroxy propyl or a mixture thereof
  • R 2 is C ⁇ -21 hydrocarbyl
  • Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof.
  • R 1 is methyl
  • R 2 is a straight Cn- ⁇ s alkyl or alkenyl chain such as coconut alkyl or mixtures thereof
  • Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
  • compositions according to the present invention may further comprise a builder system.
  • a builder system Any conventional builder system is suitable for use herein including aluminosilicate materials, silicates, polycarboxylates and fatty acids, materials such as ethylenediamine tetraacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphonic acid and diethylene triamine pentamethylenephosphonic acid.
  • phosphate builders can also be used herein.
  • Suitable builders can be an inorganic ion exchange material, commonly an inorganic hydrated aluminosilicate material, more particularly a hydrated synthetic zeolite such as hydrated zeolite A, X, B or HS.
  • SKS-6 is a crystalline layered silicate consisting of sodium silicate (Na2Si2 ⁇ 5) .
  • Suitable polycarboxylates builders for use herein include citric acid, preferably ih the form of a water-soluble salt, derivatives of succinic acid of the formula R-CH(COOH)CH2 (COOH) wherein R is C10-20 alkyl or alkenyl, preferably C12-16, or wherein R can be substituted with hydroxyl, sulfo sulfoxyl or sulfone substituents.
  • Succinate builders are preferably used in the form of their water-soluble salts, including sodium, potassium, ammonium and alkanolammonium salts.
  • polycarboxylates are oxodisuccinates and mixtures of tartrate monosuccinic and tartrate disuccinic acid such as described in US 4,663,071.
  • Especially suitable fatty acid builders for use herein are saturated or unsaturated C10-18 fatty acids, as well as the corresponding soaps.
  • Preferred saturated species have from 12 to 16 carbon atoms in the alkyl chain.
  • the preferred unsaturated fatty acid is oleic acid.
  • Another preferred builder system for liquid compositions is based on dodecenyl succinic acid.
  • Suitable water-soluble organic salts are the homo- or co- polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.
  • Polymers of this type are disclosed in GB-A-1,596,756.
  • Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000.
  • Detergency builder salts are normally included in amounts of from 10% to 80% by weight of the composition preferably from 20% to 70% and most usually from 30% to 60% by weight.
  • detergent compositions may be employed, such enzymes and stabilizers or activators therefore, soil-suspending agents soil-release agents, optical brighteners, abrasives, bactericides, tarnish inhibitors, coloring agents, and perfumes.
  • liquid compositions according to the present invention can also be in "compact form", in such case, the liquid detergent compositions according to the present invention will contain a lower amount of water, compared to conventional liquid detergents.
  • the stability of the samples were measured after several periods of storage at 21°C. The stability was determined by visual inspection of the samples assessing the flocculation of the silica/silicone particles :
  • Non-ionic surfactant alkyl alcohol ethylene oxide condensate with an average of 7 ethoxylate units and an alkyl chain length of 13 to 15 carbon.
  • a water/propylene glycol solution 60:40 water:propylene glycol.
  • the surfactant containing solution is then combined with porous hydrophobic silica (currently used Sipernat D10 ex Degussa) at ratio 1:1 up to 2.5:1 times the silica's weight ( corresponding to the silica's total pore voiu e) .
  • the solution is added in a dropwise manne - under mild stirring 1000 rpms to aid the production of a homogeneously filled silica. At this stage the product is still in powder form.
  • a variant of this step includes the addition of 5% of hydrophobic silica Aerosil R972 ex Degussa after the enzyme absorption has occured.
  • This powder is subsequently dispersed in silicone oil (polydimethylsiloxane) .
  • silicone oils with viscosities of 500, 1000, 5000, 125000 and 30000 cs. Dispersion occurs under continuous stirring with a propeller mixer at 1600 to 1850 rpm for about 3 minutes.
  • the silicone oil dispersion is finally emulsified in the detergent matrix by techniques known in art.
  • a liquid detergent composition according to the present invention is prepared, having the following compositions 15
  • compositions I and II were each supplemented by the suds controlling compositions A and B (Table I) .
  • the components of the suds controlling composition were premixed before being added to the liquid detergent compositions.
  • the stability of the samples IA, IB, IIA, IIB were determined after several weeks of storage at 21"C
  • the absorption of a surfactant into the silica greatly improves the stability of the finely dispersed silica/silicone antifoam agent in the liquid detergent composition.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Inorganic Chemistry (AREA)
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  • Degasification And Air Bubble Elimination (AREA)
PCT/US1993/004924 1992-06-06 1993-05-25 Suds controlling composition comprising silicone and silica WO1993025649A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AU43894/93A AU4389493A (en) 1992-06-06 1993-05-25 Suds controlling composition comprising silicone and silica
JP6501497A JPH07507588A (ja) 1992-06-06 1993-05-25 シリコーン及びシリカを含む起泡抑制組成物
CA002137344A CA2137344C (en) 1992-06-06 1993-05-25 Suds controlling composition comprising silicone and silica
FI945732A FI945732A (fi) 1992-06-06 1994-12-05 Vaahtoa hillitsevä koostumus, joka sisältää silikonia ja piidioksidia

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19920201649 EP0573699B1 (en) 1992-06-06 1992-06-06 Suds controlling compositions
EP92201649.8 1992-06-06

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WO1993025649A1 true WO1993025649A1 (en) 1993-12-23

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PCT/US1993/004924 WO1993025649A1 (en) 1992-06-06 1993-05-25 Suds controlling composition comprising silicone and silica
PCT/US1993/005221 WO1993025652A1 (en) 1992-06-06 1993-06-04 Stable foam-controlled liquid detergent compositions

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EP (2) EP0573699B1 (fi)
JP (2) JPH07507588A (fi)
CN (1) CN1083098A (fi)
AU (2) AU4389493A (fi)
CA (2) CA2137344C (fi)
DE (1) DE69214275T2 (fi)
ES (1) ES2092624T3 (fi)
FI (2) FI945732A (fi)
IE (1) IE930429A1 (fi)
MX (1) MX9303412A (fi)
RU (2) RU94046234A (fi)
WO (2) WO1993025649A1 (fi)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5648327A (en) * 1993-07-22 1997-07-15 The Procter & Gamble Company Stable liquid detergent compositions comprising a dispersible silicone-based suds suppressor system

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5643862A (en) * 1992-06-06 1997-07-01 The Procter & Gamble Company Stable foam-controlled liquid detergent compositions
JP3711561B2 (ja) * 1993-04-05 2005-11-02 三菱ウェルファーマ株式会社 アンチトロンビン−▲iii▼液状製剤およびその安定化方法
EP0666301A1 (en) * 1994-02-04 1995-08-09 The Procter & Gamble Company Stable liquid detergent compositions
US5636638A (en) * 1994-06-29 1997-06-10 Baxter International Inc. Electrical power amplifier for continuous cardiac output monitoring
EP0745648A3 (en) * 1995-06-01 1997-12-10 Dow Corning Corporation Stable dispersible silicone compositions
WO1997009405A2 (en) * 1995-09-05 1997-03-13 Unilever N.V. Liquid detergent composition comprising dispersed hydrophilic silica
BR9712878A (pt) 1996-11-04 2000-02-01 Novo Nordisk As Variante de enzima subtilase, processos para a identificação de uma variante de protease apresentando estabilidade autoproteolìtica e paraq a produção de uma enzima subtilase mutante e de uma variante de subtilase, sequência de dna, vetor, célula hospedeira microbiana, composição e uso de uma variante de subtilase.
US6303663B1 (en) * 1999-03-26 2001-10-16 Cognis Corporation Process for making defoaming compositions
US6569826B1 (en) 1999-10-19 2003-05-27 The Procter & Gamble Company Radical scavenger
US6566320B1 (en) 1999-10-19 2003-05-20 The Procter & Gamble Company Bleaching composition containing chromotropic compound
WO2004074419A2 (en) 2003-02-18 2004-09-02 Novozymes A/S Detergent compositions
JP5816174B2 (ja) 2009-08-06 2015-11-18 アーケマ・インコーポレイテッド 液状クリーニング組成物
JP5667759B2 (ja) * 2009-12-22 2015-02-12 東レ・ダウコーニング株式会社 液体洗剤組成物、その調製方法及びその透明化方法
WO2012075611A1 (en) * 2010-12-10 2012-06-14 The Procter & Gamble Company Laundry detergents
CN103666419B (zh) * 2013-12-04 2015-12-09 天津宁赛科技有限公司 一种油井水泥复合有机硅消泡剂
JP6661712B2 (ja) * 2018-08-15 2020-03-11 旭化成ワッカーシリコーン株式会社 シリコーン消泡剤組成物、および、シリコーン消泡剤組成物の製造方法。

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4400288A (en) * 1980-07-28 1983-08-23 The Procter & Gamble Company Detergent compositions and processes of making thereof
US4652392A (en) * 1985-07-30 1987-03-24 The Procter & Gamble Company Controlled sudsing detergent compositions
US4732694A (en) * 1983-08-27 1988-03-22 The Procter & Gamble Company Suds suppressor compositions and their use in detergent compositions
US4798679A (en) * 1987-05-11 1989-01-17 The Procter & Gamble Co. Controlled sudsing stable isotropic liquid detergent compositions
US4806266A (en) * 1985-07-25 1989-02-21 Dow Corning Ltd. Detergent foam control agents containing a silicone antifoam and a fatty alcohol
US4983316A (en) * 1988-08-04 1991-01-08 Dow Corning Corporation Dispersible silicone antifoam formulations
US5045225A (en) * 1988-12-30 1991-09-03 Lever Brothers Co., Division Of Conopco Inc. Self hydrophobing silicone/hydrocarbon antifoam compositions

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1261618B (de) * 1965-01-21 1968-02-22 Henkel & Cie Gmbh Alkalische, lagerstabile, schaumarme Reinigungs- und Spuelmittel
EP0091802B1 (en) * 1982-04-13 1987-09-30 The Procter & Gamble Company Foam-controlling detergent additive compositions and use thereof in detergent compositions
GB2220932A (en) * 1988-03-18 1990-01-24 Rhone Poulenc Chimie Anti-foam composition

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4400288A (en) * 1980-07-28 1983-08-23 The Procter & Gamble Company Detergent compositions and processes of making thereof
US4732694A (en) * 1983-08-27 1988-03-22 The Procter & Gamble Company Suds suppressor compositions and their use in detergent compositions
US4806266A (en) * 1985-07-25 1989-02-21 Dow Corning Ltd. Detergent foam control agents containing a silicone antifoam and a fatty alcohol
US4652392A (en) * 1985-07-30 1987-03-24 The Procter & Gamble Company Controlled sudsing detergent compositions
US4798679A (en) * 1987-05-11 1989-01-17 The Procter & Gamble Co. Controlled sudsing stable isotropic liquid detergent compositions
US4983316A (en) * 1988-08-04 1991-01-08 Dow Corning Corporation Dispersible silicone antifoam formulations
US5045225A (en) * 1988-12-30 1991-09-03 Lever Brothers Co., Division Of Conopco Inc. Self hydrophobing silicone/hydrocarbon antifoam compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5648327A (en) * 1993-07-22 1997-07-15 The Procter & Gamble Company Stable liquid detergent compositions comprising a dispersible silicone-based suds suppressor system

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EP0573699A1 (en) 1993-12-15
CA2137344C (en) 1999-06-22
EP0573699B1 (en) 1996-10-02
DE69214275D1 (de) 1996-11-07
RU94046375A (ru) 1996-10-10
MX9303412A (es) 1994-04-29
FI945732A0 (fi) 1994-12-05
CN1083098A (zh) 1994-03-02
CA2137343A1 (en) 1993-12-23
JPH07507588A (ja) 1995-08-24
IE930429A1 (en) 1993-12-15
ES2092624T3 (es) 1996-12-01
EP0646167A1 (en) 1995-04-05
AU4389493A (en) 1994-01-04
FI945733A (fi) 1994-12-05
FI945732A (fi) 1994-12-05
DE69214275T2 (de) 1997-04-17
WO1993025652A1 (en) 1993-12-23
CA2137344A1 (en) 1993-12-23
FI945733A0 (fi) 1994-12-05
RU94046234A (ru) 1996-10-10
JPH08502684A (ja) 1996-03-26
AU4401693A (en) 1994-01-04

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